ClinVar Miner

List of variants in gene MED12 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 114
Download table as spreadsheet
HGVS dbSNP
NM_005120.2(MED12):c.3355-16_3355-13delCTGT rs1556336608
NM_005120.2(MED12):c.3355-8dupT rs750373111
NM_005120.2(MED12):c.6276_6278dup (p.Gln2115_His2116insGln) rs748394417
NM_005120.3(MED12):c.-28G>T rs373552360
NM_005120.3(MED12):c.-47A>T rs767078113
NM_005120.3(MED12):c.100-19C>T rs930154299
NM_005120.3(MED12):c.1028C>T (p.Ser343Leu) rs764107388
NM_005120.3(MED12):c.1066C>A (p.Arg356=) rs763867883
NM_005120.3(MED12):c.1101+8_1101+9insCC rs1214824818
NM_005120.3(MED12):c.111G>A (p.Thr37=) rs1057522480
NM_005120.3(MED12):c.129A>G (p.Gln43=) rs780634712
NM_005120.3(MED12):c.1332C>T (p.Cys444=) rs746205041
NM_005120.3(MED12):c.1344T>G (p.Thr448=) rs375202766
NM_005120.3(MED12):c.1348+18G>A rs776024292
NM_005120.3(MED12):c.1349-11T>C rs775255445
NM_005120.3(MED12):c.1485+6C>T rs565198403
NM_005120.3(MED12):c.1602G>A (p.Ala534=) rs1057523461
NM_005120.3(MED12):c.1618-8T>C rs1057522084
NM_005120.3(MED12):c.1659C>T (p.Ile553=) rs763388314
NM_005120.3(MED12):c.1695T>A (p.Ile565=) rs138984044
NM_005120.3(MED12):c.1744+14C>T rs1263378137
NM_005120.3(MED12):c.1744+4C>T rs780750721
NM_005120.3(MED12):c.1745-19C>T rs1057524262
NM_005120.3(MED12):c.183C>T (p.Asn61=) rs770411750
NM_005120.3(MED12):c.1929C>T (p.Asp643=) rs758195942
NM_005120.3(MED12):c.1975-5C>T rs200891932
NM_005120.3(MED12):c.204+13T>G rs901178143
NM_005120.3(MED12):c.205-38C>T rs12850852
NM_005120.3(MED12):c.2056-20C>T rs1057521831
NM_005120.3(MED12):c.2220C>T (p.Ile740=) rs370195616
NM_005120.3(MED12):c.2613G>A (p.Gln871=) rs372344160
NM_005120.3(MED12):c.2748C>A (p.Gly916=) rs768686458
NM_005120.3(MED12):c.27C>T (p.Tyr9=) rs376743527
NM_005120.3(MED12):c.2850-7C>G rs1556336208
NM_005120.3(MED12):c.3231G>T (p.Leu1077=) rs1556336518
NM_005120.3(MED12):c.3354+26A>G rs749625903
NM_005120.3(MED12):c.3412C>A (p.Arg1138=) rs1057523906
NM_005120.3(MED12):c.3456C>T (p.Ile1152=) rs1556336642
NM_005120.3(MED12):c.3516C>A (p.Thr1172=) rs1057521581
NM_005120.3(MED12):c.3516C>G (p.Thr1172=) rs1057521581
NM_005120.3(MED12):c.3577+17T>G rs1057523979
NM_005120.3(MED12):c.3577+9C>A rs1556336775
NM_005120.3(MED12):c.3699G>A (p.Ala1233=) rs184162709
NM_005120.3(MED12):c.3797G>A (p.Arg1266His) rs587780391
NM_005120.3(MED12):c.3801C>T (p.Asn1267=) rs1057520418
NM_005120.3(MED12):c.381G>A (p.Thr127=) rs202125318
NM_005120.3(MED12):c.3843C>T (p.Tyr1281=) rs369268877
NM_005120.3(MED12):c.3930A>C (p.Pro1310=) rs5030619
NM_005120.3(MED12):c.3942T>C (p.Ser1314=) rs3810670
NM_005120.3(MED12):c.4047+14G>A rs774488297
NM_005120.3(MED12):c.4048-12C>T rs1556337459
NM_005120.3(MED12):c.4111C>T (p.Pro1371Ser) rs587778437
NM_005120.3(MED12):c.4120-12C>T rs1556337617
NM_005120.3(MED12):c.4146C>T (p.Ile1382=) rs923552252
NM_005120.3(MED12):c.4179A>C (p.Ser1393=) rs376058351
NM_005120.3(MED12):c.4299T>C (p.Ala1433=) rs763359998
NM_005120.3(MED12):c.4416-43_4416-14del rs1556337864
NM_005120.3(MED12):c.4416-48T>C rs12849277
NM_005120.3(MED12):c.4416-77CTCTT[8] rs56658066
NM_005120.3(MED12):c.4470A>G (p.Lys1490=) rs766138859
NM_005120.3(MED12):c.4488C>T (p.Arg1496=) rs531754497
NM_005120.3(MED12):c.4528-19T>C rs370859385
NM_005120.3(MED12):c.4665G>A (p.Thr1555=) rs375001801
NM_005120.3(MED12):c.4851G>A (p.Ala1617=) rs377210068
NM_005120.3(MED12):c.4863+15C>T rs778076528
NM_005120.3(MED12):c.4864-6C>T rs1018026145
NM_005120.3(MED12):c.4950G>A (p.Thr1650=) rs756839501
NM_005120.3(MED12):c.4974C>T (p.Ile1658=) rs376179450
NM_005120.3(MED12):c.5026-12T>A rs1057520901
NM_005120.3(MED12):c.5026-17T>C rs1556338729
NM_005120.3(MED12):c.5088G>A (p.Pro1696=) rs202167558
NM_005120.3(MED12):c.5103T>C (p.Ser1701=) rs762801267
NM_005120.3(MED12):c.5190G>C (p.Leu1730=) rs753355369
NM_005120.3(MED12):c.5205C>T (p.Arg1735=) rs747836622
NM_005120.3(MED12):c.5266C>T (p.Leu1756=) rs1556338815
NM_005120.3(MED12):c.5400+7G>A rs201254124
NM_005120.3(MED12):c.5401-25C>T rs41298482
NM_005120.3(MED12):c.5490A>C (p.Thr1830=) rs762466624
NM_005120.3(MED12):c.5510G>C (p.Gly1837Ala) rs200328506
NM_005120.3(MED12):c.553+12C>G rs1556334127
NM_005120.3(MED12):c.5535C>T (p.Asn1845=) rs34784349
NM_005120.3(MED12):c.5593A>G (p.Met1865Val) rs587778438
NM_005120.3(MED12):c.5650G>A (p.Gly1884Ser) rs147354926
NM_005120.3(MED12):c.5659G>A (p.Gly1887Ser) rs758621985
NM_005120.3(MED12):c.5711C>T (p.Ala1904Val) rs200663107
NM_005120.3(MED12):c.5712G>A (p.Ala1904=) rs189962028
NM_005120.3(MED12):c.5775A>G (p.Ser1925=) rs376753995
NM_005120.3(MED12):c.5805C>T (p.Ser1935=) rs201608537
NM_005120.3(MED12):c.6044+16G>C rs367904425
NM_005120.3(MED12):c.6045-24C>T rs140083803
NM_005120.3(MED12):c.6072A>T (p.Thr2024=) rs200692655
NM_005120.3(MED12):c.6150_6152GCA[4] (p.Gln2075_Gln2076del) rs769857818
NM_005120.3(MED12):c.6186_6188GCA[6] (p.Gln2076dup) rs754533796
NM_005120.3(MED12):c.6201A>G (p.Gln2067=) rs375793297
NM_005120.3(MED12):c.6208_6210CAG[8] (p.Gln2076dup) rs757160341
NM_005120.3(MED12):c.6208_6210CAG[9] (p.Gln2075_Gln2076dup) rs757160341
NM_005120.3(MED12):c.6241_6243CAG[7] (p.Gln2086dup) rs786200971
NM_005120.3(MED12):c.6267+20T>C rs1032542640
NM_005120.3(MED12):c.6279A>G (p.Gln2093=) rs1050062166
NM_005120.3(MED12):c.6279_6284ACAGCA[3] (p.Gln2114_Gln2115dup) rs761195801
NM_005120.3(MED12):c.6288_6290GCA[8] (p.Gln2115dup) rs766775649
NM_005120.3(MED12):c.6288_6290GCA[9] (p.Gln2114_Gln2115dup) rs766775649
NM_005120.3(MED12):c.6309_6314ACAGCA[1] (p.Gln2114_Gln2115del) rs764789036
NM_005120.3(MED12):c.6318_6320GCA[5] (p.Gln2115dup) rs1168018409
NM_005120.3(MED12):c.6336_6362del (p.Gln2115_Gln2123del) rs1353930135
NM_005120.3(MED12):c.6348_6359dup (p.His2116_Gln2119dup) rs398124200
NM_005120.3(MED12):c.6408+16C>T rs1057522248
NM_005120.3(MED12):c.6409-14C>A rs374791085
NM_005120.3(MED12):c.708C>G (p.Thr236=) rs34668206
NM_005120.3(MED12):c.735+15A>G rs202206536
NM_005120.3(MED12):c.736-14C>G rs373707149
NM_005120.3(MED12):c.736-4A>G rs371311763
NM_005120.3(MED12):c.736-8A>C rs62609586
NM_005120.3(MED12):c.934G>C (p.Val312Leu) rs377403264

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.